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The PHF21B gene is associated with major depression and modulates the stress response

dc.contributor.authorWong, M.-L.
dc.contributor.authorArcos-Burgos, Mauricio
dc.contributor.authorLiu, S.
dc.contributor.authorVélez, Jorge
dc.contributor.authorYu, C.
dc.contributor.authorBaune, Bernhard
dc.contributor.authorJawahar, Magdalene Catharine
dc.contributor.authorArolt, V.
dc.contributor.authorDannlowsk, Udo
dc.contributor.authorChuah, Aaron
dc.contributor.authorHuttley, Gavin
dc.contributor.authorLicinio, Julio
dc.date.accessioned2021-09-30T23:48:16Z
dc.date.available2021-09-30T23:48:16Z
dc.date.issued2017
dc.date.updated2020-11-23T11:19:20Z
dc.description.abstractMajor depressive disorder (MDD) affects around 350 million people worldwide; however, the underlying genetic basis remains largely unknown. In this study, we took into account that MDD is a gene-environment disorder, in which stress is a critical component, and used whole-genome screening of functional variants to investigate the ‘missing heritability’ in MDD. Genome-wide association studies (GWAS) using single- and multi-locus linear mixed-effect models were performed in a Los Angeles Mexican-American cohort (196 controls, 203 MDD) and in a replication European-ancestry cohort (499 controls, 473 MDD). Our analyses took into consideration the stress levels in the control populations. The Mexican-American controls, comprised primarily of recent immigrants, had high levels of stress due to acculturation issues and the European-ancestry controls with high stress levels were given higher weights in our analysis. We identified 44 common and rare functional variants associated with mild to moderate MDD in the Mexican-American cohort (genome-wide false discovery rate, FDR, <0.05), and their pathway analysis revealed that the three top overrepresented Gene Ontology (GO) processes were innate immune response, glutamate receptor signaling and detection of chemical stimulus in smell sensory perception. Rare variant analysis replicated the association of the PHF21B gene in the ethnically unrelated European-ancestry cohort. The TRPM2 gene, previously implicated in mood disorders, may also be considered replicated by our analyses. Whole-genome sequencing analyses of a subset of the cohorts revealed that European-ancestry individuals have a significantly reduced (50%) number of single nucleotide variants compared with Mexican-American individuals, and for this reason the role of rare variants may vary across populations. PHF21b variants contribute significantly to differences in the levels of expression of this gene in several brain areas, including the hippocampus. Furthermore, using an animal model of stress, we found that Phf21b hippocampal gene expression is significantly decreased in animals resilient to chronic restraint stress when compared with non-chronically stressed animals. Together, our results reveal that including stress level data enables the identification of novel rare functional variants associated with MDD.Molecular Psychiatry advance online publication, 25 October 2016; doi:10.1038/mp.2016.174.en_AU
dc.description.sponsorshipWe have been supported by grants APP1051931 and APP1070935 (MLW), and APP1060524 (BB) from the National Health and Medical Research Council (Australia), the German Research Foundation (UD, Grant FOR 2107, DA1151/5-1), NIH Grant GM61394 (JL and MLW), the German Australian Institute for Translational Medicine (SRB and JL), and institutional funds from the Australian National University and the South Australian Health and Medical Research Instituteen_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1359-4184en_AU
dc.identifier.urihttp://hdl.handle.net/1885/249099
dc.language.isoen_AUen_AU
dc.provenanceThis work is licensed under a Creative Commons AttributionNonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http:// creativecommons.org/licenses/by-nc-nd/4.0/en_AU
dc.publisherNature Publishing Groupen_AU
dc.relationhttp://purl.org/au-research/grants/nhmrc/1051931en_AU
dc.relationhttp://purl.org/au-research/grants/nhmrc/1060524en_AU
dc.relationhttp://purl.org/au-research/grants/nhmrc/1070935en_AU
dc.rights© The Author(s) 2016en_AU
dc.rights.licenseCommons AttributionNonCommercial-NoDerivs 4.0 International Licenseen_AU
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_AU
dc.sourceMolecular Psychiatryen_AU
dc.titleThe PHF21B gene is associated with major depression and modulates the stress responseen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue7en_AU
local.bibliographicCitation.lastpage1025en_AU
local.bibliographicCitation.startpage1015en_AU
local.contributor.affiliationWong, M-L, Flinders University School of Medicineen_AU
local.contributor.affiliationArcos-Burgos, Mauricio (Oscar), College of Health and Medicine, ANUen_AU
local.contributor.affiliationLiu, S, SAHMRIen_AU
local.contributor.affiliationVelez, Jorge, College of Health and Medicine, ANUen_AU
local.contributor.affiliationYu, C, SAHMRIen_AU
local.contributor.affiliationBaune, Bernhard, University of Adelaideen_AU
local.contributor.affiliationJawahar, Magdalene Catharine, University of Adelaideen_AU
local.contributor.affiliationArolt, V, University of Münsteren_AU
local.contributor.affiliationDannlowsk, Udo, University of Münsteren_AU
local.contributor.affiliationChuah, Aaron, College of Health and Medicine, ANUen_AU
local.contributor.affiliationHuttley, Gavin, College of Science, ANUen_AU
local.contributor.affiliationLicinio, Julio, College of Health and Medicine, ANUen_AU
local.contributor.authoruidArcos-Burgos, Mauricio (Oscar), u5088570en_AU
local.contributor.authoruidVelez, Jorge, u5218146en_AU
local.contributor.authoruidChuah, Aaron, u5077173en_AU
local.contributor.authoruidHuttley, Gavin, u9800703en_AU
local.contributor.authoruidLicinio, Julio, u4761348en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor060102 - Bioinformaticsen_AU
local.identifier.absfor110300 - CLINICAL SCIENCESen_AU
local.identifier.absfor110900 - NEUROSCIENCESen_AU
local.identifier.ariespublicationU3488905xPUB25002en_AU
local.identifier.citationvolume22en_AU
local.identifier.doi10.1038/mp.2016.174en_AU
local.identifier.scopusID2-s2.0-84992365606
local.identifier.thomsonID000403911900010
local.publisher.urlhttp://www.nature.com/mp/en_AU
local.type.statusPublished Versionen_AU

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